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Joint Bone Spine. 2010 Jul;77(4):355-7. doi: 10.1016/j.jbspin.2010.03.007. Epub 2010 May 13.

Familiar ochronotic arthropathy-caused by a gene mutation traced three hundred years.

Author information

1
Department of Orthopedics, Faculty of Medicine, University of Szeged, 6725, Semmelweis Street 6, Szeged, Hungary. tothk@orto.szote.u-szeged.hu

Abstract

Authors trace an ochronotic Hungarian family, which moved from Slovakia to Hungary 300 years ago. As the family members lived in a relatively close village community the gene mutation had been survived silently for ages before the clinical symptoms developed. Family tree analysis could detect with the use of allele specific PCR amplification-the p.G161R mutation of the homogentisic acid 1,2-dioxygenase (HGD) gene, which resulted in a specific genotype appearing in the Slovak population. We found a heterozygote member of this family who has children with an alkaptonuria-homozygote and known-heterozygote genotypes so there would be a high risk of alkaptonuria in their offsprings. Therefore genetic counselling is highly recommended to minimize the risk factors.

PMID:
20462779
DOI:
10.1016/j.jbspin.2010.03.007
[Indexed for MEDLINE]

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